Urea 40 Percent Cream

Manufacturer
Bryant Ranch Prepack
Effective date
2026-03-27
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
101
Source
full-release
Hydrated at
2026-05-31 22:11:54

Label at a glance#

ProductUrea 40 Percent
Active ingredientUREA
Label structure10 sections

Dosage and administration

Use as directed by your physician. See label booklet for full Prescribing Information.

Label contents#

Full prescribing information#

DESCRIPTION:

DESCRIPTION SECTION

INGREDIENTS: Each gram

of Urea Cream 40%

contains Urea 40% and the

following inactive

ingredients: Carbomer,

Cetearyl Alcohol, Glycerin,

Glyceryl Stearate SE,

Mineral Oil, Purified Water,

White Petrolatum.

descdesc

CLINICAL PHARMACOLOGY:

CLINICAL PHARMACOLOGY SECTION

Urea gently dissolves the intercellular matrix which results in loosening the horny layer of skin and shedding scaly skin at regular intervals, thereby softening hyperkeratotic areas of the skin.

Pharmacokinetics:

PHARMACOKINETICS SECTION

The mechanism of action of topically applied urea is not yet known.

INDICATIONS:

INDICATIONS & USAGE SECTION

This product is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, xerosis, ichthyosis, skin cracks and fissures, dermatitis, eczema, psoriasis, keratoses and calluses.

CONTRAINDICATIONS:

CONTRAINDICATIONS SECTION

This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.

WARNINGS:

WARNINGS SECTION

FOREXTERNALUSEONLY.NOTFOR OPHTHALMIC USE. KEEP OUT OF REACH OF CHILDREN.

Avoid contact with eyes, lips and mucous membranes.

General:

GENERAL PRECAUTIONS SECTION

This product is to be used as directed by a physician and should not be used to treat any condition other than that for which it was prescribed. If redness or irritation occurs, discontinue use and consult a physician.

Information for Patients:

INFORMATION FOR PATIENTS SECTION

Patients should discontinue the use of this product if the condition becomes worse or if a rash develops in the area being treated or elsewhere. Avoid contact with eyes, lips and mucous membranes.

Carcinogenesis, Mutagenesis and Impairment of Fertility:

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Long-term animal studies for carcinogenic potential have not been performed on this product to date. Studies on reproduction and fertility also have not been performed.

Pregnancy:

PREGNANCY SECTION

Category C. Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus.

Nursing Mothers:

NURSING MOTHERS SECTION

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this product is administered to a nursing woman.

ADVERSE REACTIONS:

ADVERSE REACTIONS SECTION

Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product.

DOSAGE AND ADMINISTRATION:

DOSAGE & ADMINISTRATION SECTION

Use as
directed by your physician.
See label booklet for full
Prescribing Information.

STORAGE:

SAFE HANDLING WARNING SECTION

Store at room
temperature 15°C-30°C
(59°F-86°F).
Protect from freezing.
Keep bottle tightly closed.

HOW SUPPLIED:

HOW SUPPLIED SECTION

This product is supplied in the following size:

NDC 72162-1668-2: 7 oz (198.4 g)
Repackaged/Relabeled by:
Bryant Ranch Prepack
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Urea Cream 40% #198.4

Label
Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198342urea 40 % Topical CreamPSN101
198342urea 400 MG/ML Topical CreamSCD101
198342urea 40 % Topical CreamSY101

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1287216216682lbl721621668.jpg
Data codeData Matrix0100363629103317211444981724013110LOT42832lbl721621668.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1668-2Urea 40 Percent198.4 g in 1 BOTTLECREAM198.4101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1668-2GM - Gram72162-16680e212dcb-7fef-4482-a9eb-178289e1562412025-02-10
58657-487-01GM - Gram58657-4876cc9ad67-4027-4a1a-977f-6cf12e22639412022-02-07
58657-487-03GM - Gram58657-487e3820119-276c-4c8a-8c62-164a4b76514a12022-02-07
58657-487-07GM - Gram58657-487b02e37c2-ec4f-48de-b296-a5fc2cf8097d12022-02-07

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72162-166872162-1668-2
58657-487

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Urea 40 PercentUREABryant Ranch Prepackee06a590-a104-4e97-b66c-cd37869038a52026-03-27Warnings, Adverse reactionsExact identifier
ndc (package): 72162-1668-2
ndc (product): 72162-1668
ndc11 (package): 72162166802
spl id: ce18811d-88e5-4660-aef6-be4b5b0a24eb
spl set id: ee06a590-a104-4e97-b66c-cd37869038a5
Urea 40 PercentUREAMethod Pharmaceuticals, LLCd35b75e1-937d-ebc4-e053-2a95a90ac0d82026-02-12Warnings, Adverse reactionsExact identifier
ndc (product): 58657-487

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.